Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2225361생성일: 2026년 10월 27일
Amoxapine → Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinecarboxylic Acid Ester
https://huagongshe.com/reaction/2225361
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Amoxapine | HCID 2170 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Ethyl 4-(2-Chlorodibenz[b,f][1,4]oxazepin-11-yl)-1-piperazinecarboxylic Acid Ester | HCID 19004074 | 97% |
반응 단계
A mixture of 2.20 g of 2-chloro-11-(1-piperazinyl)dibenz[b,f][1,4]oxazepine, 0.76 g of ethyl chloroformate and 0.97 g of potassium carbonate in 20 ml of N,N-dimethylformamide was stirred at 80° C. for 3 hrs. Ice water was added to the reaction mixture and extracted with ether. The etheral layer was washed with water, dried and concentrated. The residue was chromatographed on silica gel using a mixture of n-hexane and ethyl acetate (1:2) as eluents to give 2.62 g of colorless crystals, which were recrystallized from isopropyl ether to give colorless prisms, mp 121.5°-122.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05344828 |
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| 출처 데이터셋 | uspto-grants-1994_09 |
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| ORD ID | ord-3a7d3ae34f4c4c6cb85cf3f4240a1400 |
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| 출처 메모 | uspto-grants-1994_09 |
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